NDC 0591-0781 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0591-0781 |
| Marketing Category | / |
| Marketing Category | NDA authorized generic |
| Application Number | NDA016131 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1990-10-01 |
| Marketing End Date | 2018-06-30 |